Hernàndez Pando R, Aguilar L D, Infante E, Cataldi A, Bigi F, Martin C, Gicquel B
Experimental Pathology Section, Pathology Department, National Institute of Medical Sciences and Nutrition Salvador Zubiràn, Vasco de Quiroga 15, Tlalpan, Mexico City, Mexico.
Tuberculosis (Edinb). 2006 May-Jul;86(3-4):203-10. doi: 10.1016/j.tube.2006.01.022. Epub 2006 Mar 20.
Given the variable protective efficacy generated by Mycobacterium bovis BCG (Bacillus Calmette-Guérin), there is a concerted effort worldwide to develop better vaccines that could be used to reduce the burden of tuberculosis. Rational attenuated mutants of Mycobacterium tuberculosis are vaccine candidates that offer some potential in this area. In this paper, we will discuss the molecular methods used to generate mutant mycobacteria, as well as the results obtained with some of these strains, in terms of attenuation, immunogenicity and level of protection, when compared with the conventional BCG vaccine in diverse animal models. Tuberculosis vaccine candidates based on safe and live mycobacterial mutants could be promising candidates.
鉴于牛分枝杆菌卡介苗(Bacillus Calmette-Guérin)所产生的保护效力存在差异,全球正在齐心协力研发更优疫苗,以减轻结核病负担。结核分枝杆菌的合理减毒突变体是有望在这一领域发挥作用的疫苗候选物。在本文中,我们将讨论用于产生突变分枝杆菌的分子方法,以及其中一些菌株在不同动物模型中与传统卡介苗相比,在减毒、免疫原性和保护水平方面所取得的结果。基于安全的活分枝杆菌突变体的结核病疫苗候选物可能是很有前景的候选者。